Literature DB >> 33237907

Characterisation of 22445 patients attending UK emergency departments with suspected COVID-19 infection: Observational cohort study.

Steve Goodacre1, Ben Thomas1, Ellen Lee1, Laura Sutton1, Amanda Loban1, Simon Waterhouse1, Richard Simmonds1, Katie Biggs1, Carl Marincowitz1, Jose Schutter1, Sarah Connelly1, Elena Sheldon1, Jamie Hall1, Emma Young1, Andrew Bentley2, Kirsty Challen3, Chris Fitzsimmons4, Tim Harris5, Fiona Lecky1, Andrew Lee1, Ian Maconochie6, Darren Walter7.   

Abstract

BACKGROUND: Hospital emergency departments play a crucial role in the initial assessment and management of suspected COVID-19 infection. This needs to be guided by studies of people presenting with suspected COVID-19, including those admitted and discharged, and those who do not ultimately have COVID-19 confirmed. We aimed to characterise patients attending emergency departments with suspected COVID-19, including subgroups based on sex, ethnicity and COVID-19 test results. METHODS AND
FINDINGS: We undertook a mixed prospective and retrospective observational cohort study in 70 emergency departments across the United Kingdom (UK). We collected presenting data from 22445 people attending with suspected COVID-19 between 26 March 2020 and 28 May 2020. Outcomes were admission to hospital, COVID-19 result, organ support (respiratory, cardiovascular or renal), and death, by record review at 30 days. Mean age was 58.4 years, 11200 (50.4%) were female and 11034 (49.6%) male. Adults (age >16 years) were acutely unwell (median NEWS2 score of 4), frequently had limited performance status (46.9%) and had high rates of admission (67.1%), COVID-19 positivity (31.2%), organ support (9.8%) and death (15.5%). Children had much lower rates of admission (27.4%), COVID-19 positivity (1.2%), organ support (1.4%) and death (0.3%). Similar numbers of men and women presented to the ED, but men were more likely to be admitted (72.9% v 61.4%), require organ support (12.2% v 7.7%) and die (18.2% v 13.0%). Black or Asian adults tended to be younger than White adults (median age 54, 50 and 67 years), were less likely to have impaired performance status (43.1%, 26.8% and 51.6%), be admitted to hospital (60.8%, 57.3%, 69.6%) or die (11.6%, 11.2%, 16.4%), but were more likely to require organ support (15.9%, 14.3%, 8.9%) or have a positive COVID-19 test (40.8%, 42.1%, 30.0%). Adults admitted with suspected and confirmed COVID-19 had similar age, performance status and comorbidities (except chronic lung disease) to those who did not have COVID-19 confirmed, but were much more likely to need organ support (22.2% v 8.9%) or die (32.1% v 15.5%).
CONCLUSIONS: Important differences exist between patient groups presenting to the emergency department with suspected COVID-19. Adults and children differ markedly and require different approaches to emergency triage. Admission and adverse outcome rates among adults suggest that policies to avoid unnecessary ED attendance achieved their aim. Subsequent COVID-19 confirmation confers a worse prognosis and greater need for organ support. REGISTRATION: ISRCTN registry, ISRCTN56149622, http://www.isrctn.com/ISRCTN28342533.

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Mesh:

Year:  2020        PMID: 33237907      PMCID: PMC7688143          DOI: 10.1371/journal.pone.0240206

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

Hospital emergency departments (ED) have played a crucial role during the COVID-19 pandemic in receiving acutely ill patients, determining the need for admission and critical care, and providing emergency treatment. International [1, 2] and national [3-6] guidelines have been developed for the emergency management of suspected COVID-19. Studies of hospitalised cases with COVID-19 [7-10] inform the emergency management of suspected COVID-19 but have important limitations. First, patients typically present with suspected rather than proven COVID-19. This presentation includes many patients with characteristics of COVID-19, who need urgent care, but do not ultimately have the virus. Second, emergency management involves differentiating those with severe illness who require hospital admission from those with mild or moderate illness who can be managed at home. Appropriate management of this heterogeneous population is an important challenge that needs to be informed by relevant data. The Pandemic Respiratory Infection Emergency System Triage (PRIEST) study collected data from consecutive patients attending EDs across the UK with suspected COVID-19. We aimed to characterise patients attending EDs with suspected COVID-19, including subgroups based on sex, ethnicity and COVID-19 results.

Materials and methods

The PRIEST study was originally set up and piloted as the Pandemic Influenza Triage in the Emergency Department (PAINTED) study as part of the UK National Institute for Health Research (NIHR) pandemic portfolio of studies to be activated in the event of an influenza pandemic [11, 12]. It was developed into the PRIEST study and expanded to include other respiratory infections in response to the emerging COVID-19 pandemic. We undertook an observational cohort study of adults and children attending the ED with suspected COVID-19 infection. Patients were included if the assessing clinician recorded that the patient had suspected COVID-19 in the ED records or completed a standardised assessment form for suspected COVID-19 patients. The clinical diagnostic criteria for COVID-19 during the study were of fever (≥ 37.8°C) and at least one of the following respiratory symptoms, which must be of acute onset: persistent cough (with or without sputum), hoarseness, nasal discharge or congestion, shortness of breath, sore throat, wheezing, sneezing. We did not seek consent to collect data but information about the study was provided in the ED and patients could withdraw their data at their request. Patients with multiple presentations to hospital were only included once, using data from the first presentation identified by research staff. Baseline characteristics at presentation to the ED were recorded prospectively, using a standardised assessment form developed and piloted for the PAINTED study [12] that doubled as a clinical record (SF_S1 Appendix: Standardised Data Collection Form), or retrospectively, through research staff extracting data onto the standardised form using the clinical records. Research staff collected follow-up data onto a standardised follow-up form (SDF_S2 Appendix: Follow-up Form) using clinical records up to 30 days after presentation. They then entered data onto a secure online database managed by the Sheffield Clinical Trials Research Unit (CTRU). Patients who died or required respiratory, cardiovascular or renal support were classified as having an adverse outcome. Patients who survived to 30 days without requiring respiratory, cardiovascular or renal support were classified as having no adverse outcome. Respiratory support was defined as any intervention to protect the patient’s airway or assist their ventilation, including non-invasive ventilation or acute administration of continuous positive airway pressure. It did not include supplemental oxygen alone or nebulised bronchodilators. Cardiovascular support was defined as any intervention to maintain organ perfusion, such as inotropic drugs, or invasively monitor cardiovascular status, such as central venous pressure or pulmonary artery pressure monitoring, or arterial blood pressure monitoring. It did not include peripheral intravenous cannulation or fluid administration. Renal support was defined as any intervention to assist renal function, such as haemofiltration, haemodialysis or peritoneal dialysis. It did not include intravenous fluid administration. The sample size was determined by the size and severity of the pandemic, but was originally planned to involve recruiting 20,000 patients across 40 sites. This was expected to include 200 with an adverse outcome, based on a 1% prevalence of adverse outcome in a previous study undertaken during the 2009 H1N1 pandemic. This paper presents a descriptive analysis of the cohort. We calculated a National Early Warning Score (2nd version, NEWS2) for adults, to provide an overall assessment of acute illness severity on a scale from zero to 20, based on respiratory rate, oxygen saturation, systolic blood pressure, heart rate, level of consciousness and temperature [13]. We calculated a modified Paediatric Observation Priority Score (POPS) for children for the same purpose, with a scale from zero to 14, based on respiratory rate, oxygen saturation, heart rate, level of consciousness, temperature, breathing and past medical history (excluding the gut feeling parameter) [14]. We undertook descriptive analysis of subgroups based on age, sex and ethnicity. We also compared the characteristics and outcomes of admitted patients with positive COVID-19 testing to those with negative or no testing.

Ethical approval

The North West—Haydock Research Ethics Committee gave a favourable opinion on the PAINTED study on 25 June 2012 (reference 12/NW/0303) and on the updated PRIEST study on 23rd March 2020. The Confidentiality Advisory Group of the Health Research Authority granted approval to collect data without patient consent in line with Section 251 of the National Health Service Act 2006.

Patient and public involvement

The Sheffield Emergency Care Forum (SECF) is a public representative group interested in emergency care research [15]. Members of SECF advised on the development of the PRIEST study and two members joined the Study Steering Committee. Patients were not involved in the recruitment to and conduct of the study. We are unable to disseminate the findings to study participants directly.

Results

The PRIEST study recruited 22484 patients from 70 EDs across 53 sites between 26 March 2020 and 28 May 2020. We included 22445 in the analysis after excluding 39 who requested withdrawal of their data. The mean age was 58.4 years, 11200 (50.4%) were female, 11034 (49.6%) male (211 missing), and ethnicity was 15198 (84.7%) UK/Irish/other white, 1150 (6.4%) Asian, 692 (3.9%) Black/African/Caribbean, 328 (1.8%) mixed/multiple ethnic groups, 570 (3.2%) other ethnic groups and 4507 unknown (missing data or preferring not to say). After ED assessment COVID-19 was considered the most likely diagnosis for 14400 (67.2% of those with non-missing data). Fig 1 shows that hourly presentations between 11:00 and 18:00 were around four times the night-time rate.
Fig 1

Time of presentation to the ED.

Table 1 shows the baseline characteristics, presenting features and physiology of adults and children in the cohort, and Table 2 shows the admission decisions and adverse outcomes for adults and children.
Table 1

Baseline characteristics, presenting features and physiology of adults (N = 20908) and children (N = 1530)†.

CharacteristicStatistic/levelAdultsChildren
Age (years)N209081530
Mean (SD)62.4 (19.7)3.6 (4.2)
Median (IQR)64 (48,79)2 (0,6)
SexMissing19318
Male10209 (49.3%)821 (54.3%)
Female10506 (50.7%)691 (45.7%)
EthnicityMissing/prefer not to say4215290
UK/Irish/other white14243 (85.3%)950 (76.6%)
Asian1044 (6.3%)106 (8.5%)
Black/African/Caribbean640 (3.8%)52 (4.2%)
Mixed/multiple ethnic groups247 (1.5%)81 (6.5%)
Other519 (3.1%)51 (4.1%)
Presenting featuresCough12994 (62.1%)580 (37.9%)
Shortness of breath15586 (74.5%)314 (20.5%)
Fever10282 (49.2%)1222 (79.9%)
Symptom duration (days)N188901442
Mean (SD)7.9 (8.9)4.3 (5.9)
Median (IQR)5 (2,10)2 (1,5)
Heart rate (beats/min)N204771482
Mean (SD)94.9 (21.6)137.2 (28.4)
Median (IQR)93 (80,108)138 (118,157)
Respiratory rate (breaths/min)N203631473
Mean (SD)23.3 (7)33.1 (10.3)
Median (IQR)22 (18,26)32 (26,40)
Systolic BP (mmHg)N20315376
Mean (SD)134.6 (24.9)107.9 (15.2)
Median (IQR)133 (118,149)109 (98,117)
Diastolic BP (mmHg)N20228366
Mean (SD)78.2 (16.1)65.3 (12.4)
Median (IQR)78 (68,88)64 (58,73)
Temperature (°C)N202481485
Mean (SD)37.1 (1.1)37.5 (1.1)
Median (IQR)37 (36.4,37.8)37.4 (36.7,38.3)
Oxygen saturation (%)N206491498
Mean (SD)94.7 (6.8)97.7 (3.1)
Median (IQR)96 (94,98)98 (97,99)
Glasgow Coma ScaleN15434506
Mean (SD)14.6 (1.4)14.9 (0.9)
Median (IQR)15 (15,15)15 (15,15)
AVPUMissing2391120
Alert17580 (94.9%)1394 (98.9%)
Verbal640 (3.5%)11 (0.8%)
Pain183 (1%)3 (0.2%)
Unresponsive114 (0.6%)2 (0.1%)

†N = 7 omitted due to missing age

Table 2

Outcomes of adults (N = 20908) and children (N = 1530).

OutcomeLevelAdult N (%)Child N (%)
Admitted at initial assessmentMissing453
No6866 (32.9%)1109 (72.6%)
Yes13997 (67.1%)418 (27.4%)
Respiratory pathogenCOVID-196521 (31.2%)19 (1.2%)
Influenza27 (0.1%)2 (0.1%)
Other1721 (8.2%)237 (15.5%)
None identified12639 (60.5%)1272 (83.1%)
Mortality statusMissing203
Alive17642 (84.5%)1523 (99.7%)
Dead3246 (15.5%)4 (0.3%)
 Death with organ support*693 (21.3%)0 (0%)
 Death with no organ support*2553 (78.7%)4 (100%)
Organ supportRespiratory1944 (9.3%)18 (1.2%)
Cardiovascular517 (2.5%)8 (0.5%)
Renal218 (1%)2 (0.1%)
Any2058 (9.8%)22 (1.4%)

*Denominator = total deaths in category

†N = 7 omitted due to missing age *Denominator = total deaths in category Adults with suspected COVID-19 were acutely unwell, with a lower IQR oxygen saturation of 94% and an upper IQR respiratory rate of 26/minute, and had high rates of admission (67.1%), organ support (9.8%) and death (15.5%). Children with suspected COVID-19 also presented with abnormal physiology, but had low rates of admission, organ support and mortality. Adults tended to present with cough and breathlessness, while children tended to present with fever. Very few children had a positive test for COVID-19, compared with almost a third of adults. Fig 2 shows the NEWS2 score for adults and Fig 3 shows the POPS score for children. The median (inter-quartile range [IQR]) NEWS2 score was 4 (2, 7) for adults and the median POPS score was 1 (1, 3) for children.
Fig 2

Adult patients NEWS2 scores.

Fig 3

Child patient POPS scores.

Table 3 shows that adults with suspected COVID-19 had substantial co-morbidities (30.8% with hypertension and 19.7% with diabetes) and almost half were recorded as having some limitation of normal activities. A substantial proportion (19.3%) had a Do Not Attempt Resuscitation decision recorded on or before the day of presentation.
Table 3

Co-morbidities, performance status and Do Not Attempt Resuscitation decisions for adults (N = 20908).

CharacteristicLevelN (%)
ComorbiditiesHypertension6437 (30.8%)
Heart Disease4702 (22.5%)
Diabetes4129 (19.7%)
Other chronic lung disease3767 (18%)
Asthma3410 (16.3%)
Renal impairment1934 (9.3%)
Active malignancy1120 (5.4%)
Immunosuppression631 (3%)
Steroid therapy557 (2.7%)
No Chronic disease5798 (27.7%)
Performance statusMissing1080
Unrestricted normal activity10541 (53.2%)
Limited strenuous activity, can do light2373 (12%)
Limited activity, can self care2781 (14%)
Limited self care2649 (13.4%)
Bed/chair bound, no self care1484 (7.5%)
DNAR in place after ED assessment4029 (19.3%)
Table 4 shows that men tended to be older than women, have slightly more severe illness, and were more likely to have hypertension, heart disease, diabetes or chronic lung disease, while women were more likely to have asthma. Men and women attended the ED in similar numbers, but men were more likely to be admitted, have positive COVID-19 testing, require organ support and die.
Table 4

Characteristics and outcomes of male (N = 10209) and female (N = 10506) adults†.

CharacteristicStatistic/levelAdult menAdult women
Age (years)N1020910506
Mean (SD)64 (18.3)60.8 (20.9)
Median (IQR)66 (51,79)61 (45,79)
Presenting featuresCough6406 (62.7%)6473 (61.6%)
Shortness of breath7646 (74.9%)7811 (74.3%)
Fever5224 (51.2%)4969 (47.3%)
Symptom duration (days)N92169501
Mean (SD)7.6 (8.5)8.3 (9.2)
Median (IQR)5 (2,10)5 (2,10)
Respiratory rate (breaths/min)N995110228
Mean (SD)23.7 (7.3)22.8 (6.7)
Median (IQR)22 (18,27)21 (18,26)
Oxygen saturation (%)N1009410367
Mean (SD)94.2 (7)95.1 (6.6)
Median (IQR)96 (93,98)97 (94,98)
NEWS2 scoreN1011810304
Mean (SD)4.7 (3.4)4.1 (3.2)
Median (IQR)4 (2,7)4 (1,6)
ComorbiditiesHypertension3356 (32.9%)3013 (28.7%)
Heart Disease2718 (26.6%)1945 (18.5%)
Diabetes2343 (23%)1747 (16.6%)
Other chronic lung disease1981 (19.4%)1760 (16.8%)
Asthma1261 (12.4%)2117 (20.2%)
Renal impairment1029 (10.1%)888 (8.5%)
Active malignancy659 (6.5%)453 (4.3%)
Immunosuppression294 (2.9%)333 (3.2%)
Steroid therapy248 (2.4%)305 (2.9%)
No Chronic disease2659 (26%)3080 (29.3%)
Performance statusMissing530539
Unrestricted normal activity5005 (51.7%)5437 (54.6%)
Limited strenuous activity, can do light1216 (12.6%)1134 (11.4%)
Limited activity, can self care1420 (14.7%)1339 (13.4%)
Limited self care1315 (13.6%)1308 (13.1%)
Bed/chair bound, no self care723 (7.5%)749 (7.5%)
Admitted at initial assessmentMissing2223
No2765 (27.1%)4043 (38.6%)
Yes7422 (72.9%)6440 (61.4%)
Respiratory pathogenCOVID-193612 (35.4%)2851 (27.1%)
Influenza (pandemic or seasonal)10 (0.1%)17 (0.2%)
Other809 (7.9%)902 (8.6%)
None identified5778 (56.6%)6736 (64.1%)
Mortality statusMissing911
Alive8341 (81.8%)9132 (87%)
Dead1859 (18.2%)1363 (13%)
 Death with organ support*439 (23.6%)250 (18.3%)
 Death with no organ support*1420 (76.4%)1113 (81.7%)
Organ supportRespiratory1165 (11.4%)769 (7.3%)
Cardiovascular360 (3.5%)151 (1.4%)
Renal155 (1.5%)61 (0.6%)
Any1241 (12.2%)805 (7.7%)

†N = 193 omitted due to missing sex

*Denominator = total deaths in category

†N = 193 omitted due to missing sex *Denominator = total deaths in category Table 5 reports the characteristics and outcomes of adults in different ethnic groups. Black or Asian adults tended to be younger than White adults, were less likely to have impaired performance status, be admitted to hospital or die, but were more likely to require organ support or have a positive COVID-19 test. Comorbidities also varied between ethnic groups.
Table 5

Characteristics and outcomes of different ethnic groups among adults.

CharacteristicStatistic/levelUK/Irish/ other whiteAsianBlack/ African/ CaribbeanMixed/ Multiple groupsOtherUnknown
Age (years)N1424310446402475194215
Mean (SD)64.5 (19.5)52.8 (17.8)55 (17.7)52.8 (19.3)51.2 (18.5)60.6 (19.7)
Median (IQR)67 (51,81)50 (40,66)54 (41.5,67)52 (36,69)48 (38,64)61 (46,77)
SexMissing1291164538
Male6858 (48.6%)531 (51.4%)309 (48.7%)104 (42.8%)269 (52.3%)2138 (51.2%)
Female7256 (51.4%)502 (48.6%)325 (51.3%)139 (57.2%)245 (47.7%)2039 (48.8%)
Presenting featuresCough8749 (61.4%)717 (68.7%)386 (60.3%)155 (62.8%)342 (65.9%)2646 (62.8%)
Shortness of breath10662 (74.9%)765 (73.3%)442 (69.1%)178 (72.1%)388 (74.8%)3151 (74.8%)
Fever6756 (47.4%)650 (62.3%)329 (51.4%)127 (51.4%)288 (55.5%)2132 (50.6%)
Symptom duration (days)N128919886012324943684
Mean (SD)7.6 (8.7)9.3 (8.9)9.1 (9.5)8.8 (8.8)8.7 (7.7)8.3 (9.5)
Median (IQR)5 (2,10)7 (3,13)7 (3,14)7 (3,10.5)7 (3,12)6 (2,10)
Respiratory rate (breaths/min)N1389810136172395024094
Mean (SD)23.2 (6.8)24.2 (8.2)23.7 (7.8)22.5 (7.2)22.4 (6.6)23.3 (7.1)
Median (IQR)22 (18,26)22 (18,28)21 (18,28)20 (18,25)20 (18,24)21 (18,26)
Oxygen saturation (%)N1407910316342455134147
Mean (SD)94.5 (6.9)95 (7.6)95.3 (7)95.6 (5.9)95.5 (6.4)94.8 (6.4)
Median (IQR)96 (94,98)97 (95,98)97 (95,99)97 (95,99)97 (95,98)96 (94,98)
NEWS2 scoreN1406210216322415094146
Mean (SD)4.5 (3.3)4.2 (3.3)4.1 (3.3)3.8 (3.3)3.7 (3.2)4.4 (3.3)
Median (IQR)4 (2,7)4 (1,6)4 (1,6)3 (1,6)3 (1,6)4 (2,7)
ComorbiditiesHypertension4576 (32.1%)338 (32.4%)253 (39.5%)61 (24.7%)105 (20.2%)1104 (26.2%)
Heart Disease3563 (25%)158 (15.1%)66 (10.3%)28 (11.3%)56 (10.8%)831 (19.7%)
Diabetes2743 (19.3%)334 (32%)175 (27.3%)59 (23.9%)67 (12.9%)751 (17.8%)
Other chronic lung disease2938 (20.6%)70 (6.7%)45 (7%)29 (11.7%)47 (9.1%)638 (15.1%)
Asthma2400 (16.9%)160 (15.3%)99 (15.5%)36 (14.6%)63 (12.1%)652 (15.5%)
Renal impairment1415 (9.9%)86 (8.2%)63 (9.8%)17 (6.9%)23 (4.4%)330 (7.8%)
Active malignancy865 (6.1%)26 (2.5%)22 (3.4%)7 (2.8%)12 (2.3%)188 (4.5%)
Immunosuppression445 (3.1%)33 (3.2%)29 (4.5%)7 (2.8%)13 (2.5%)104 (2.5%)
Steroid therapy414 (2.9%)19 (1.8%)14 (2.2%)4 (1.6%)15 (2.9%)91 (2.2%)
No Chronic disease3452 (24.2%)380 (36.4%)189 (29.5%)97 (39.3%)257 (49.5%)1423 (33.8%)
Performance statusMissing7062813621306
Unrestricted normal activity6549 (48.4%)744 (73.2%)356 (56.8%)180 (74.7%)367 (73.7%)2345 (60%)
Limited strenuous activity, can do light1755 (13%)84 (8.3%)81 (12.9%)22 (9.1%)40 (8%)391 (10%)
Limited activity, can self care2095 (15.5%)79 (7.8%)70 (11.2%)23 (9.5%)36 (7.2%)478 (12.2%)
Limited self care2058 (15.2%)50 (4.9%)54 (8.6%)9 (3.7%)32 (6.4%)446 (11.4%)
Bed/chair bound, no self care1080 (8%)59 (5.8%)66 (10.5%)7 (2.9%)23 (4.6%)249 (6.4%)
Admitted at initial assessmentMissing22100022
No4329 (30.4%)445 (42.7%)251 (39.2%)108 (43.7%)262 (50.5%)1472 (35.1%)
Yes9892 (69.6%)598 (57.3%)389 (60.8%)139 (56.3%)257 (49.5%)2722 (64.9%)
Respiratory pathogenCOVID-194278 (30%)440 (42.1%)261 (40.8%)68 (27.5%)170 (32.8%)1304 (30.9%)
Influenza (pandemic or seasonal)23 (0.2%)1 (0.1%)0 (0%)0 (0%)0 (0%)3 (0.1%)
Other1361 (9.6%)65 (6.2%)29 (4.5%)16 (6.5%)19 (3.7%)231 (5.5%)
None identified8581 (60.2%)538 (51.5%)350 (54.7%)163 (66%)330 (63.6%)2677 (63.5%)
Mortality statusMissing3000017
Alive11903 (83.6%)927 (88.8%)566 (88.4%)221 (89.5%)473 (91.1%)3552 (84.6%)
Dead2337 (16.4%)117 (11.2%)74 (11.6%)26 (10.5%)46 (8.9%)646 (15.4%)
 Death with organ support*442 (18.9%)40 (34.2%)30 (40.5%)13 (50%)17 (37%)151 (23.4%)
 Death with no organ support*1895 (81.1%)77 (65.8%)44 (59.5%)13 (50%)29 (63%)495 (76.6%)
Organ supportRespiratory1189 (8.3%)139 (13.3%)93 (14.5%)31 (12.6%)53 (10.2%)439 (10.4%)
Cardiovascular278 (2%)58 (5.6%)45 (7%)5 (2%)14 (2.7%)117 (2.8%)
Renal115 (0.8%)22 (2.1%)31 (4.8%)3 (1.2%)5 (1%)42 (1%)
Any1264 (8.9%)149 (14.3%)102 (15.9%)34 (13.8%)53 (10.2%)456 (10.8%)

*Denominator = total deaths in category

*Denominator = total deaths in category Table 6 shows the characteristics and outcomes of admitted adults with subsequent positive COVID-19 testing and admitted patients with negative or no testing. Age, presenting characteristics, performance status and comorbidities (except chronic lung disease) did not differ markedly between the two groups, but adults with confirmed COVID-19 were more likely to die or require organ support.
Table 6

Characteristics and outcomes of admitted adult patients with (N = 5768) and without (N = 8229) positive COVID-19 test.

CharacteristicStatistic/levelCOVID-19 positiveCOVID-19 negative or not tested
Age (years)N57688229
Mean (SD)69.8 (16.6)68.4 (17.8)
Median (IQR)73 (58,83)72 (57,82)
SexMissing5382
Male3282 (57.4%)4140 (50.8%)
Female2433 (42.6%)4007 (49.2%)
Presenting featuresCough3722 (64.5%)4633 (56.3%)
Shortness of breath4390 (76.1%)6158 (74.8%)
Fever3425 (59.4%)3629 (44.1%)
Symptom duration (days)N51997278
Mean (SD)6.9 (6.3)7 (8.9)
Median (IQR)6 (2,10)3 (2,8)
Respiratory rate (breaths/min)N56348060
Mean (SD)25.6 (7.8)23.9 (6.9)
Median (IQR)24 (20,29)22 (19,28)
Oxygen saturation (%)N57108152
Mean (SD)92.7 (7.8)94.1 (7)
Median (IQR)95 (91,97)96 (93,98)
NEWS2 scoreN57118146
Mean (SD)6.1 (3.2)5.2 (3.2)
Median (IQR)6 (4,8)5 (3,7)
ComorbiditiesHypertension2251 (39%)3000 (36.5%)
Heart Disease1605 (27.8%)2457 (29.9%)
Diabetes1591 (27.6%)1885 (22.9%)
Other chronic lung disease978 (17%)2189 (26.6%)
Asthma770 (13.3%)1276 (15.5%)
Renal impairment769 (13.3%)959 (11.7%)
Active malignancy282 (4.9%)693 (8.4%)
Immunosuppression181 (3.1%)309 (3.8%)
Steroid therapy160 (2.8%)288 (3.5%)
No Chronic disease1158 (20.1%)1406 (17.1%)
Performance statusMissing232504
Unrestricted normal activity2224 (40.2%)2989 (38.7%)
Limited strenuous activity, can do light605 (10.9%)1160 (15%)
Limited activity, can self care856 (15.5%)1625 (21%)
Limited self care1128 (20.4%)1286 (16.6%)
Bed/chair bound, no self care723 (13.1%)665 (8.6%)
Mortality statusMissing01
Alive3918 (67.9%)6952 (84.5%)
Dead1850 (32.1%)1276 (15.5%)
 Death with organ support*471 (25.5%)208 (16.3%)
 Death with no organ support*1379 (74.5%)1068 (83.7%)
Organ supportRespiratory1235 (21.4%)661 (8%)
Cardiovascular379 (6.6%)128 (1.6%)
Renal151 (2.6%)65 (0.8%)
Any1278 (22.2%)729 (8.9%)

*Denominator = total deaths in category

*Denominator = total deaths in category

Discussion

Our study describes the presentation of suspected COVID-19 to EDs across the United Kingdom over the first wave of the pandemic. This large, generalizable cohort allows us to characterise the challenge faced by EDs, identify important differences between demographic groups and guide planning for future emergency care. Adults presenting to the ED with suspected COVID-19 tended to have severe illness, with relatively high NEWS2 scores and abnormal respiratory physiology, and a correspondingly high rate of admission and adverse outcome. Children had a much lower rate of admission and a very low rate of adverse outcome. Adults were also much more likely to have confirmed COVID-19 than children. Suspected COVID-19 in adults and children could therefore be considered as different entities, requiring different approaches to triage, diagnosis and management. A number of policies were implemented during the pandemic to reduce unnecessary ED attendances with suspected COVID-19. The UK National Health Service advised people with suspected COVID-19 to use the online or telephone NHS111 service rather than attend the ED directly. Some ambulance services avoided transferring people to the ED if they did not have features of severe disease. Our findings suggest that these approaches resulted in an adult ED population with severe illness and high rate of admission. Further research is underway as part of the PRIEST study to determine whether this was achieved at the expense of delayed hospital admission for some cases. Adults admitted with suspected COVID-19 that was subsequently confirmed were more than twice as likely to die or receive organ support as those who did not have COVID-19 confirmed, despite having similar age, performance status and comorbidities (expect chronic lung disease). Admission with COVID-19 therefore confers a markedly worse prognosis compared to similar presentations. We are only aware of one other study comparing ED presentations in this way—a small single centre study from San Francisco showing no difference in mortality [16]. Men and women presented to the ED with suspected COVID-19 in almost equal numbers, but men were more likely to be admitted, have positive COVID-19 testing, receive organ support and die. This may be explained by age and comorbidities. Previous studies have shown a male majority of around 60% among admitted patients [7–10, 17–19]. Petrilli et al included patients managed as outpatients or discharged from the ED in their cohort and report similar findings to us, with an equal ratio presenting but men more likely to be admitted [20]. Black or Asian adults tended to be younger than White adults, had less impairment of performance status, and were less likely to be admitted to hospital or die, but were more likely to require organ support or have a positive COVID-19 test. A recent systematic review [21] suggested Black or Asian people are at an increased risk of acquiring COVID-19 and a greater risk of worse clinical outcomes compared to White people. Most studies in the review were from the United States, where social imbalances and inequalities in the access to health care may explain these increased risks. Harrison et al studied admitted patients with a high likelihood of COVID-19 infection across UK hospitals over the same time period as our study and showed that higher mortality among the White population was explained by age on multivariable analysis [22]. In contrast, Price-Heywood et al found that high mortality associated with Black ethnicity in Louisiana was explained by sociodemographic and clinical characteristics [23], while Petrelli et al showed that Hispanic ethnicity in New York was associated with an increased risk of hospital admission but not of critical illness [20]. These findings suggest a complex interaction between underlying demographics and comorbidities, susceptibility to COVID-19 and use of health services may explain differences between ethnic groups. Our study is based on a large and generalizable cohort covering the first wave of the pandemic, but has some limitations. A combination of prospective and retrospective data collection was used, and infection control measures limited our ability to collect data directly from patients. Reliance on clinical records may have underestimated the prevalence of some presenting features and co-morbidities, and resulted in missing data for some variables. Selection of cases was based on subjective clinical judgement that COVID-19 was a suspected diagnosis, which may have been applied in a variable manner between clinicians and between sites. Our analysis was limited to describing the cohort rather than using multivariable analysis to explain the observed differences between groups. We felt that the latter analysis would need to be based on a clear theoretical rationale and inclusion of appropriate covariates, which would be beyond the scope of this study. Finally, the use of our data to guide planning of emergency care may be limited by changes in the characteristics of patients presenting in future waves of the pandemic. Further research is therefore required to determine the characteristics of patients in future waves.

Conclusion

We have shown important differences between patient groups presenting to the ED with suspected COVID-19. Adults and children differ markedly and require different approaches to emergency triage. Admission and adverse outcome rates among adults suggest that policies to avoid unnecessary ED attendance achieved their aim. Subsequent COVID-19 confirmation confers a worse prognosis and greater need for organ support.

Standardised data collection form.

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Follow-up form.

(PDF) Click here for additional data file.

Study steering committee.

(DOCX) Click here for additional data file.

Site research staff.

(DOCX) Click here for additional data file.

Supporting research staff.

(DOCX) Click here for additional data file.

Transfer Alert

This paper was transferred from another journal. As a result, its full editorial history (including decision letters, peer reviews and author responses) may not be present. 15 Sep 2020 PONE-D-20-25198 Characterisation of 22446 patients attending UK emergency departments with suspected COVID-19 infection: Observational cohort study PLOS ONE Dear Dr. Goodacre, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. Please submit your revised manuscript by the 5th of October. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript: A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'. A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'. An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter. If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols We look forward to receiving your revised manuscript. Kind regards, Walter R. Taylor Academic Editor PLOS ONE Journal Requirements: When submitting your revision, we need you to address these additional requirements. 1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. 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We will update your Data Availability statement on your behalf to reflect the information you provide. 3.Thank you for stating the following in the Competing Interests section: [All authors declare grant funding to their employing institutions from the National Institute for Health Research, as outlined under financial disclosure information. SG is Deputy Director of the NIHR Health Technology Assessment (HTA) Programme, which funded the study, and chairs the NIHR HTA commissioning commitee.]. Please confirm that this does not alter your adherence to all PLOS ONE policies on sharing data and materials, by including the following statement: "This does not alter our adherence to  PLOS ONE policies on sharing data and materials.” (as detailed online in our guide for authors http://journals.plos.org/plosone/s/competing-interests).  If there are restrictions on sharing of data and/or materials, please state these. Please note that we cannot proceed with consideration of your article until this information has been declared. Please include your updated Competing Interests statement in your cover letter; we will change the online submission form on your behalf. Please know it is PLOS ONE policy for corresponding authors to declare, on behalf of all authors, all potential competing interests for the purposes of transparency. PLOS defines a competing interest as anything that interferes with, or could reasonably be perceived as interfering with, the full and objective presentation, peer review, editorial decision-making, or publication of research or non-research articles submitted to one of the journals. Competing interests can be financial or non-financial, professional, or personal. Competing interests can arise in relationship to an organization or another person. Please follow this link to our website for more details on competing interests: http://journals.plos.org/plosone/s/competing-interests 4. One of the noted authors is a group or consortium [The PRIEST Research Group]. In addition to naming the author group, please list the individual authors and affiliations within this group in the acknowledgments section of your manuscript. Please also indicate clearly a lead author for this group along with a contact email address. 5. Please respond by return e-mail with an updated version of your manuscript to amend either the abstract on the online submission form or the abstract in the manuscript so that they are identical. We can make any changes on your behalf. 6. Please include captions for your Supporting Information files at the end of your manuscript, and update any in-text citations to match accordingly. Please see our Supporting Information guidelines for more Additional Editor Comments (if provided): Dear Dr. Goodacre, I have received comments from one reviewer. This reviewer has raised some interesting points and I look forward to seeing your responses. yours sincerely, Walter Taylor. Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes ********** 3. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes ********** 4. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes ********** 5. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: The manuscript presented by Goodacre and colleagues adds important epidemiological information to the understanding of the SARS-CoV-2 epidemic in the UK. The authors analysed the clinical data of 22446 patients admitted with suspected COVID-19 to 70 emergency rooms in the UK from March 26th until May 28th 2020. In summery - Male sex as a risk factor for a more severe cause of COVID-19 - COVID-19 results in a more severe course than other respiratory diseases even when the groups have similar rates of comorbidities in the beginning. - And to some interest, ethnical differences which (to my knowledge) can’t be explained by biological facts. Black and Asian adults were roughly 15 years younger, had a better performance status, were less likely to be admitted to hospital and were less likely to die. Nevertheless, they had a higher rate of COVID-19 positive tests and needed more organ support. For me the last point is of importance. The authors state that Black and Asian patients might have a higher risk for a more severe COVID-19 course. But the review article they cite (Ref. 21) may not be optimal to prove this claim. Most studies included in this review reporting differences in outcome depending on ethnicity were from the US. Due to fundamental differences in the US and UK health care systems, the result of these studies are rather a surrogate for social imbalances and inequalities in the access to health care than a prove for biological differences. The study is well executed and the presentation of the results are fine. However, in the discussion the authors claim that their study allows to “…guide planning for future emergency care.” I would like to question this in at least in part. Because the manuscript describes the first wave. Presumable some of the parameters will be the same during the ongoing pandemic but others will change; the introduction of the virus will happen through other routes, precaution measures for populations at risk are still in place and pandemic response will be based on the experience of the past. How an epidemic may change you see for example in Germany, the average age of patients diagnosed with CODIV-19 dropped from 52 years in May 2020 to 32 years in August (national surveillance data from the Robert Koch Institute). Hospital and ICU admission rates dropped from ≈ 10% and 4% to 3% and >1% respectively. ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: No [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. 20 Sep 2020 Thank you for considering our paper and for the reviewer’s thoughtful comments. We have revised our paper to address these comments and we provide our responses below. The amendments are marked using track changes in the revised manuscript. We have also made a very small amendment to the numbers in the manuscript as a result of identifying a duplicated case. The reduction from 22446 to 22445 cases resulted in no significant change to the reported findings. The authors state that Black and Asian patients might have a higher risk for a more severe COVID-19 course. But the review article they cite (Ref. 21) may not be optimal to prove this claim. Most studies included in this review reporting differences in outcome depending on ethnicity were from the US. Due to fundamental differences in the US and UK health care systems, the result of these studies are rather a surrogate for social imbalances and inequalities in the access to health care than a proof for biological differences. Thank you for highlighting this. We have added a sentence to the discussion to make this point. We have also added a reference for the Harrison study, which was undertaken in the UK. The study is well executed and the presentation of the results are fine. However, in the discussion the authors claim that their study allows to “…guide planning for future emergency care.” I would like to question this in at least in part. Because the manuscript describes the first wave. Presumable some of the parameters will be the same during the ongoing pandemic but others will change; the introduction of the virus will happen through other routes, precaution measures for populations at risk are still in place and pandemic response will be based on the experience of the past. How an epidemic may change you see for example in Germany, the average age of patients diagnosed with CODIV-19 dropped from 52 years in May 2020 to 32 years in August (national surveillance data from the Robert Koch Institute). Hospital and ICU admission rates dropped from ≈ 10% and 4% to 3% and >1% respectively. Thank you for highlighting this issue. We have added a couple of sentences to the discussion to acknowledge this limitation and identify the need for further research to characterise patients presenting in future waves of the pandemic. 23 Sep 2020 Characterisation of 22445 patients attending UK emergency departments with suspected COVID-19 infection: Observational cohort study PONE-D-20-25198R1 Dear Dr. Goodacre,, We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements. Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication. An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. Kind regards, Walter R. Taylor Academic Editor PLOS ONE Additional Editor Comments (optional): None Reviewers' comments: 17 Nov 2020 PONE-D-20-25198R1 Characterisation of 22445 patients attending UK emergency departments with suspected COVID-19 infection: Observational cohort study Dear Dr. Goodacre: I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. If we can help with anything else, please email us at plosone@plos.org. Thank you for submitting your work to PLOS ONE and supporting open access. Kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Walter R. Taylor Academic Editor PLOS ONE
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